CDC Warns of Higher Potential for Rare Childhood Virus AFM This Year

Kimberly Zapata
·3-min read
Young girl with curly brown hair wearing an orange top leans against a wall and looks directly at the camera
Young girl with curly brown hair wearing an orange top leans against a wall and looks directly at the camera

What happened: The Centers for Disease Control and Prevention (CDC) has a disconcerting warning for parents and caregivers: There may be another outbreak of acute flaccid myelitis — or AFM — this fall.

AFM is rare. Only 633 cases have been confirmed since the CDC began tracking it in August 2014. Cases seem to spike every two to four years. That said, acute flaccid myelitis is serious. The neurological condition can cause temporary or permanent paralysis. Many of the symptoms of AFM are also similar to those of COVID-19. For example, AFM can present as a fever or a respiratory illness.

Dr. Jennifer Ashton told Good Morning America parents should be prepared to act if they see any signs of this disease. “If they [parents] see signs or symptoms, especially like limb weakness, they should bring their child to an emergency room immediately… the hospital is the place to be.”

Related:Download The Mighty app to connect in real time with people who can relate to what you're going through.

The Frontlines: Many have noticed a striking similarity between AFM and the poliovirus, a once-common but since eradicated childhood illness. Polio killed and paralyzed millions in the 1940s and ‘50s. In addition to fever, limb weakness and respiratory distress, AFM presents in a few other ways, including:

  • Pain or numbness

  • Gait difficulty

  • Back or neck pain

  • Difficulty swallowing

  • Headaches are also common.

As we head into these critical next months, CDC is taking necessary steps to help clinicians better recognize signs and symptoms of AFM in children. Recognition and early diagnosis are critical. CDC and public health partners have strengthened early disease detection systems, a vital step toward rapid treatment and rehabilitation for children with AFM. — Robert Redfield, M.D., CDC Director

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A Mighty Voice: Our contributor, Sarah Todd Hammer, shared what her life was like when she was diagnosed with AFM. “On April 19, 2010, I was in ballet class when I got a severe headache. I was going to head home when my arms and hands fell limp at my sides, paralyzed. I walked to the car with my mom to go to an urgent care center, but when we arrived 10 minutes later, I couldn’t walk (even though my legs still moved).” You can submit your first person story, too.

Related:How We're Embracing a 'New' Quality of Life for Our Medically Fragile Child During COVID-19

Add your voice:

A banner promoting The Mighty's new Undiagnosed group on The Mighty mobile app. The banner reads, Not diagnosed, but still experiencing very real symptoms? In the Undiagnosed group, we support and encourage each other while we search for answers. Click to join.
A banner promoting The Mighty's new Undiagnosed group on The Mighty mobile app. The banner reads, Not diagnosed, but still experiencing very real symptoms? In the Undiagnosed group, we support and encourage each other while we search for answers. Click to join.

Other things to know: While AFM is a relatively new condition, there is a lot doctors, researchers and scientists can — and will — learn. Here’s what we know so far:

To learn more about AFM: For the most up-to-date information about AFM, including outbreak information and possible causes, follow the Centers for Disease Control and Prevention here.

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